Matsuyama S, Sakiyama H, Nei K, Tanaka C
Department of Pharmacoloy, Kobe University School of Medicine, Japan.
J Pharmacol Exp Ther. 1996 Mar;276(3):989-95.
We investigated the existence and the function of 5-hydroxytryptamine(4) (5-HT4) receptors and the effect of TKS159, a novel agonist of 5-HT4 receptor, on guinea pig stomach. The mechanical activity and the release of [3H]ACh were measured using preparations of muscle layers attached to intramural plexus from guinea pig stomach. 5-HT in the presence of 1 microM methysergide, 1 microM ketanserin and 1 microM granisetron, 5-methoxytryptamine or TKS159 enhanced the electrical transmural stimulation-evoked contraction and [3H]ACh release in strips of the stomach in a concentration-dependent manner. This enhancement by 5-HT, 5-methoxytryptamine or TKS159 was antagonized by SDZ 205-557 or atropine. Cisapride, metoclopramide and TKS159 enhanced the electrical transmural stimulation-evoked contraction and release of [3H]ACh in a concentration-dependent manner. We conclude that the pharmacological characteristics of the receptor, which mediates contraction of the guinea pig stomach by the activation of cholinergic nerves, are consistent with its being of the putative 5-HT4 receptor type and that TKS159 is an agonist at 5-HT4 receptors.
我们研究了5-羟色胺(4)(5-HT4)受体的存在及其功能,以及新型5-HT4受体激动剂TKS159对豚鼠胃的影响。使用豚鼠胃壁内神经丛附着的肌层制备物来测量机械活性和[3H]乙酰胆碱(ACh)的释放。在存在1微摩尔麦角新碱、1微摩尔酮色林和1微摩尔格拉司琼的情况下,5-羟色胺、5-甲氧基色胺或TKS159以浓度依赖性方式增强胃条中电跨壁刺激诱发的收缩和[3H]ACh释放。5-羟色胺、5-甲氧基色胺或TKS159的这种增强作用被SDZ 205-557或阿托品拮抗。西沙必利、甲氧氯普胺和TKS159以浓度依赖性方式增强电跨壁刺激诱发的收缩和[3H]ACh释放。我们得出结论,通过激活胆碱能神经介导豚鼠胃收缩的受体的药理学特性与其为假定的5-HT4受体类型一致,并且TKS159是5-HT4受体的激动剂。